CA3117180A1 - Proppant particles formed from slurry droplets and method of use - Google Patents
Proppant particles formed from slurry droplets and method of useInfo
- Publication number
- CA3117180A1 CA3117180A1 CA3117180A CA3117180A CA3117180A1 CA 3117180 A1 CA3117180 A1 CA 3117180A1 CA 3117180 A CA3117180 A CA 3117180A CA 3117180 A CA3117180 A CA 3117180A CA 3117180 A1 CA3117180 A1 CA 3117180A1
- Authority
- CA
- Canada
- Prior art keywords
- proppant
- pellets
- sintered
- alumina
- slurry
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 74
- 239000002245 particle Substances 0.000 title claims abstract description 64
- 239000002002 slurry Substances 0.000 title abstract description 41
- 239000000919 ceramic Substances 0.000 claims abstract description 31
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 46
- 239000011148 porous material Substances 0.000 claims description 30
- 239000005995 Aluminium silicate Substances 0.000 claims description 21
- 235000012211 aluminium silicate Nutrition 0.000 claims description 21
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 21
- 239000012530 fluid Substances 0.000 claims description 19
- 229910001570 bauxite Inorganic materials 0.000 claims description 15
- 230000003746 surface roughness Effects 0.000 claims description 9
- 230000015572 biosynthetic process Effects 0.000 claims description 8
- 229910010293 ceramic material Inorganic materials 0.000 claims description 6
- 230000008569 process Effects 0.000 abstract description 46
- 238000005266 casting Methods 0.000 abstract description 20
- 239000000463 material Substances 0.000 abstract description 9
- 239000008188 pellet Substances 0.000 description 85
- 230000035699 permeability Effects 0.000 description 27
- 238000007580 dry-mixing Methods 0.000 description 19
- 238000005345 coagulation Methods 0.000 description 16
- 230000015271 coagulation Effects 0.000 description 16
- 239000007788 liquid Substances 0.000 description 16
- 239000007921 spray Substances 0.000 description 16
- 230000007774 longterm Effects 0.000 description 10
- 239000002994 raw material Substances 0.000 description 10
- 238000009826 distribution Methods 0.000 description 9
- 239000012295 chemical reaction liquid Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000012495 reaction gas Substances 0.000 description 7
- 235000012431 wafers Nutrition 0.000 description 7
- 238000005755 formation reaction Methods 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000004005 microsphere Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000005086 pumping Methods 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229940072056 alginate Drugs 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- CEYULKASIQJZGP-UHFFFAOYSA-L disodium;2-(carboxymethyl)-2-hydroxybutanedioate Chemical compound [Na+].[Na+].[O-]C(=O)CC(O)(C(=O)O)CC([O-])=O CEYULKASIQJZGP-UHFFFAOYSA-L 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003758 nuclear fuel Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 238000011020 pilot scale process Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 238000005550 wet granulation Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/02—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops
- B01J2/04—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops in a gaseous medium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/18—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic using a vibrating apparatus
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/66—Compositions based on water or polar solvents
- C09K8/68—Compositions based on water or polar solvents containing organic compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/80—Compositions for reinforcing fractures, e.g. compositions of proppants used to keep the fractures open
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Powder Metallurgy (AREA)
Abstract
Proppant material for hydraulic fracturing is provided. The particles of the proppant are formed by drip casting. A slurry of finely divided ceramic particles is flowed through nozzles and formed into droplets under the influence of vibration. Uniform sized, smooth surface, spherical green particles are formed. The green particles are dried and sintered to form the proppant. The proppant is used in the process of hydraulic fracturing of wells.
Description
PROPPANT PARTICLES FORMED FROM SLURRY
DROPLETS AND METHOD OF USE
BACKGROUND OF INVENTION
1. FIELD OF THE INVENTION
[0001] This invention relates to hydraulic fracturing of subterranean formations in the earth.
More particularly, sintered ceramic proppant particles formed from vibration-induced dripping from a nozzle of a slurry of finely-divided ceramic material are provided, along with a method of use of the particles.
DROPLETS AND METHOD OF USE
BACKGROUND OF INVENTION
1. FIELD OF THE INVENTION
[0001] This invention relates to hydraulic fracturing of subterranean formations in the earth.
More particularly, sintered ceramic proppant particles formed from vibration-induced dripping from a nozzle of a slurry of finely-divided ceramic material are provided, along with a method of use of the particles.
2. Description of Related Art [0002] Hydraulic fracturing is a process of pumping liquids down a well and into a subterranean founation at high rate and pressure, such that a fracture is formed in the rock around the well. After pumping a liquid volume sufficient to widen the fracture adequately, solid particles, called "proppant," are added to the liquid. After pumping is completed, the well is opened for production of hydrocarbons. The production rate of fluid from the well is usually significantly increased after the fracturing treatment. Vast improvements in the hydraulic fracturing process have been developed since the process was originally patented in 1949. (U.S. Pat. Nos. 2,596,843 and 2,596,844)
[0003] The material first used for proppant in hydraulic fracturing of wells was silica sand.
As wells became deeper, sand was found to have inadequate strength. In deep wells, stress of the earth causes the sand to crush and become much less effective in increasing the production rate of a well.
As wells became deeper, sand was found to have inadequate strength. In deep wells, stress of the earth causes the sand to crush and become much less effective in increasing the production rate of a well.
[0004] Synthetic proppant materials were developed to provide higher strength proppants.
The original synthetic sintered proppant was sintered bauxite. In later years, a variety of ceramic raw materials have been used to make sintered ceramic proppants, including bauxite containing lesser amounts of alumina and clay minerals, such as kaolin.
Generally, it has been found that the strength of ceramic particles increases with the amount of alumina in the particle, all other factors remaining constant.
The original synthetic sintered proppant was sintered bauxite. In later years, a variety of ceramic raw materials have been used to make sintered ceramic proppants, including bauxite containing lesser amounts of alumina and clay minerals, such as kaolin.
Generally, it has been found that the strength of ceramic particles increases with the amount of alumina in the particle, all other factors remaining constant.
[0005] A general procedure for making synthetic proppant particles is to obtain the ceramic raw material, grind it to a fine powder, form it into pellets (called "green"
pellets), and sinter the green pellets in a kiln. The final product is ceramic pellets in the size range suitable for proppants ¨ from about 70 mesh to 12 mesh (0.008 inch to 0.067 inch).
Different sizes of pellets are used depending on well conditions.
Date Recue/Date Received 2021-05-05
pellets), and sinter the green pellets in a kiln. The final product is ceramic pellets in the size range suitable for proppants ¨ from about 70 mesh to 12 mesh (0.008 inch to 0.067 inch).
Different sizes of pellets are used depending on well conditions.
Date Recue/Date Received 2021-05-05
[0006] A variety of processes for forming the pellets of a proppant have been proposed. In early work, U.S. Pat. No. 4,427,068 describes a process for forming sintered ceramic pellets by adding dry powders of clay and alumina, bauxite, or mixtures to a high intensity mixer (hereinafter referred to as "dry mixing method"). Powdered fine grain ceramic starting ingredients (ceramic raw materials) are stirred to form a dry homogenous mixture. Then, sufficient water is added to cause agglomeration of the fine starting dust particles to form small composite spherical pellets from the powder. Continued mixing time is allowed in order to grow small pellets to the desired size. A broad range of sizes is produced during the pellet- forming stage. A preferred mixing device is obtained from Eirich Machines, Inc., and is known as the Eirich mixer. The resulting pellets are dried and sintered into the final proppant particles. Much of the ceramic proppant made in industry in past years has been made with this process of forming pellets.
[0007] U.S. Pat. No. 4,440,866 discloses an alternative process for producing pellets that are sintered to produce high strength pellets. A continuous spray/granulation of an aqueous binder containing aluminous ore suspension is used to form granules that are subsequently sintered (hereinafter referred to as "spray fluidized bed method"). All steps of this process may be carried out in a continuous manner. An aqueous suspension containing the ceramic raw material is continuously atomized and fed into a layer of already partially dried small starting dust particles (often called seeds) that are fluidized in a stream of hot drying air. The aqueous ceramic raw material suspension is continuously sprayed and dried onto the seed particles until the desired finished green particle diameter is achieved.
Particles produced in this process have a size range that is less broad than those typically produced by the dry mixing method of U.S. Pat. No. 4,427,068 but are still of sufficient variation as to require further processing. Particles are continuously recovered from the layer and they are separated from oversized and undersized product fractions. Material is continuously recycled in the stream of drying air. This spray fluidized bed process has also been used to produce large amounts of ceramic proppants in industry.
Particles produced in this process have a size range that is less broad than those typically produced by the dry mixing method of U.S. Pat. No. 4,427,068 but are still of sufficient variation as to require further processing. Particles are continuously recovered from the layer and they are separated from oversized and undersized product fractions. Material is continuously recycled in the stream of drying air. This spray fluidized bed process has also been used to produce large amounts of ceramic proppants in industry.
[0008] The pellet-forming methods described above have intrinsic limitations.
The dry mixing process produces an extremely wide range of green pellet sizes due to the random nature of the agitation of the rotor and pan. The spray fluidized bed process produces a somewhat tighter green pellet size distribution but still a much wider distribution than desired. These processes require extensive screening and recycling during the manufacturing process. Under the best manufacturing conditions about 30% of green particles must be Date Recue/Date Received 2021-05-05 recycled through the pellet-forming process. Both the dry mixing and spray fluidized bed processes also produce a random distribution of pore sizes in pellets, including a small percentage of very large pores that significantly degrade pellet strength.
Strength of the sintered pellets is a primary consideration, because if the pellets break under high stress in a fracture, the flow capacity of the fracture is decreased and the hydraulic fracturing treatment is less effective. The sphericity and surface smoothness of particles produced by these processes are also important, with high sphericity and a very smooth surface traditionally being most desirable. All of these characteristics are strongly affected by the pellet-forming method.
The dry mixing process produces an extremely wide range of green pellet sizes due to the random nature of the agitation of the rotor and pan. The spray fluidized bed process produces a somewhat tighter green pellet size distribution but still a much wider distribution than desired. These processes require extensive screening and recycling during the manufacturing process. Under the best manufacturing conditions about 30% of green particles must be Date Recue/Date Received 2021-05-05 recycled through the pellet-forming process. Both the dry mixing and spray fluidized bed processes also produce a random distribution of pore sizes in pellets, including a small percentage of very large pores that significantly degrade pellet strength.
Strength of the sintered pellets is a primary consideration, because if the pellets break under high stress in a fracture, the flow capacity of the fracture is decreased and the hydraulic fracturing treatment is less effective. The sphericity and surface smoothness of particles produced by these processes are also important, with high sphericity and a very smooth surface traditionally being most desirable. All of these characteristics are strongly affected by the pellet-forming method.
[0009] U.S. Pub. No. 2006/0016598 discloses a list of pellet-forming techniques that may be used for ceramic proppant formation, including agglomeration, spray granulation, wet granulation, extruding and pelletizing, vibration induced dripping according to U.S. Pat. No.
5,500,162, spray nozzle-formed droplets and selective agglomeration. U.S. Pat.
No.
5,500,162 discloses producing microspheres by vibration-provoked dripping of a chemical solution through a nozzle plate, wherein the falling drops form an envelope surrounded from all sides by flowing reaction gas. The liquid chemical solution has no or low (i.e. 20% or less) solid particles at the time it enters the nozzle plate, exits the nozzle plate, and passes through the first free fall section. The reaction gas is required to cause the precipitation (gelling) of small solid particles (typically sub-micron) in the liquid drops as they fall through the second free fall zone, and thereafter fall into a reaction liquid to further gel. The reaction gas is necessary to cause the liquid to partially gel prior to entering the reaction liquid, and the droplets are decelerated into the liquid through a foam or the reaction liquid is directed onto the falling drops tangentially in the same direction in which the droplets are falling. These two features of falling through reaction gas and decelerating the droplets into foam are required to insure the droplets are partially gelled during a sol-gel reaction and therefore not deformed, for example flattened, when they strike the reaction liquid. The reaction gas is sucked away inside or outside the envelope. The method according to the invention can be used to produce, for example, aluminum oxide spheres up to the diameter of mm.
5,500,162, spray nozzle-formed droplets and selective agglomeration. U.S. Pat.
No.
5,500,162 discloses producing microspheres by vibration-provoked dripping of a chemical solution through a nozzle plate, wherein the falling drops form an envelope surrounded from all sides by flowing reaction gas. The liquid chemical solution has no or low (i.e. 20% or less) solid particles at the time it enters the nozzle plate, exits the nozzle plate, and passes through the first free fall section. The reaction gas is required to cause the precipitation (gelling) of small solid particles (typically sub-micron) in the liquid drops as they fall through the second free fall zone, and thereafter fall into a reaction liquid to further gel. The reaction gas is necessary to cause the liquid to partially gel prior to entering the reaction liquid, and the droplets are decelerated into the liquid through a foam or the reaction liquid is directed onto the falling drops tangentially in the same direction in which the droplets are falling. These two features of falling through reaction gas and decelerating the droplets into foam are required to insure the droplets are partially gelled during a sol-gel reaction and therefore not deformed, for example flattened, when they strike the reaction liquid. The reaction gas is sucked away inside or outside the envelope. The method according to the invention can be used to produce, for example, aluminum oxide spheres up to the diameter of mm.
[0010] Vibration-induced dripping, herein called "drip casting," was originally developed to produce nuclear fuel pellets. Since then it has been adapted to produce a very wide variety of metal and ceramic microspheres, such as grinding media and catalyst supports.
Primarily, it has been used in the food and pharmaceuticals industries. The drip casting process is Date Recue/Date Received 2021-05-05 described on the website and in sales literature of Brace GmbH. Examples of "microspheres"
formed by drip casting of different materials are also provided. U.S. Pat. No.
6,197,073 discloses a process for producing aluminum oxide beads from an acid aluminum oxide sol or acid aluminum oxide suspension by flowing the suspension through a vibrating nozzle plate to form droplets and pre-solidifying the droplets with gaseous ammonia and then coagulating the droplets in an ammonia solution. The mechanical strength of ceramic particles formed by sintering the drip cast particles was not a factor in any of the materials used in these references.
[00111 It is known that to produce ceramic proppant particles having maximum strength for a given ceramic material, the particles must contain minimum porosity, and the pores present must be kept as small as possible, since the strength of a given proppant particle is limited by its largest pore. What is needed is a method of forming green ceramic particles that can be fired to have reduced pore size and therefore maximum strength for use as a proppant.
Preferably, the particles should be spherical, have a smooth surface and have uniform size. A
method for forming the green particles without recycling of the undesired size fraction of green ceramic pellets is also needed.
BRIEF SUMMARY OF THE INVENTION
[0012] A method for forming proppant pellets from a slurry of ceramic raw materials is provided. The pellets produced have superior strength to prior proppant pellets made from a variety of ceramic raw materials using prior art pellet-forming methods.
Uniform sized spherical pellets having a smooth surface may be made in commercial quantities. The particles are used in hydraulic fracturing treatments of wells.
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S) [0013] FIG. 1 is a sketch showing the principles of the pellet-forming apparatus for proppant pellets disclosed herein.
[0014] FIG. 2 is a sketch showing a single nozzle forming droplets from a slurry stream.
[0015] FIG. 3 is a sketch showing a multi-nozzle plate forming droplets from a slurry stream.
[0016] FIG. 4a is a showing of an alumina particle made of drip casting.
[0017] FIG. 4b is a showing of an alumina particle made by an Eirich mixer.
[0018] FIG. 4c is a showing of a bauxite particle made by drip casting.
[0019] FIG. 4d is a showing of a bauxite particle made by an Eirich mixer.
Date Recue/Date Received 2021-05-05 [0020] FIG. 4e shows a kaolin particle made by drip casting.
[0021] FIG. 4f shows a kaolin particle made by a scale fluidized bed process.
[0022] FIG. 5 is a graph of long term permeability as a function of stress of alumina pellets formed by the pellet-forming apparatus disclosed herein and by the prior art dry mixing process using an Eirich mixer.
[0023] FIG. 6 is a frequency plot of pore size for particles of kaolin made by the method disclosed herein and by the prior art spray fluidized bed method.
[0024] FIG. 7 is a graph of long term permeability data for proppant having different alumina contents and made by different processes.
[0025] FIG. 8 is a graph of long-term permeability data for proppant having different alumina contents and made by different processes.
DETAILED DESCRIPTION
[0026] Referring to FIG. 1, pellet-forming apparatus 10 having a single nozzle is shown to illustrate the principles of the method disclosed herein, which is commonly called "drip casting." Nozzle 12 receives slurry 15from feed tank 14, which contains the ceramic raw materials suspended in water. Pressure applied to feed tank 14 by pressure supply system 16 causes slurry to flow through nozzle 12 at a selected rate ¨
preferably in laminar flow. Below nozzle 12 is coagulation vessel 17, which receives the droplets.
Vibrator unit 18 is connected to nozzle 12 and is used to supply pressure pulses to the nozzle or directly in the slurry flowing to the nozzle. The resulting vibration of the slurry flow through the nozzle causes the stream exiting the nozzle 12 to break into droplets of unifoun size. As droplets fall toward coagulation vessel 17, surface tension effects tend to form the droplets into spheres. Spherical particles are formed without the necessity of a sol-gel reaction, reaction gas free fall zone, foamed layer of reaction liquid or reaction liquid directed onto the droplets prior to entering the reaction liquid bath.
[0027] FIG. 2 shows details of slurry 15 exiting nozzle 12 and breaking into drops. Surface tension of the slurry drives the drops toward minimum surface area, which is acquired in a spherical shape, as they fall toward coagulation vessel 17. The distance of fall is preferably selected to be great enough to allow the droplets to become spherical before entering a liquid in vessel 17.
[0028] Slurry 15 from feed tank 14 contains a finely ground (0.01 ¨ 50 microns in size) mineral or processed powder capable of producing a strong ceramic material after sintering, a Date Recue/Date Received 2021-05-05 proper amount of dispersant necessary for keeping the solid particles in the slurry well separated, water, and a reactant that will react with a component in liquid 19 in coagulation vessel 17 to form a semi-solid or insoluble compound. The solids content of the slurries may range from about 25% to about 75%. The viscosity of the slurries will normally be from 1 to 1,000 centipoise, but may be higher. Lower viscosity of the slurry aids in improving droplet formation and formation of spherical particles and is an essential part of the invention claimed. Optimization of the dispersant type and concentration will reduce viscosity.
Dispersants may be selected based on cost, availability and effectiveness in reducing viscosity of a selected slurry. Dispersants that may be used to reduce the viscosity of slurries include sodium silicate, ammonium polyacrylate, sodium polymethacrylate, sodium citrate sodium polysulfonate and hexametaphosphate.
[0029] The commonly used reactant chemical in the slurry in feed tank 14 is sodium alginate.
This is a naturally occurring polysaccharide that is soluble in water as the sodium salt but is cross-linked to form a gel as the calcium salt. Alginate is typically added to the slurry at levels of 0.1% to 1.0% (weight percent alginate solid to total slurry).
Coagulation tank 17 normally contains a coagulation liquid 19 which gels the reactant chemical in the slurry 15.
The commonly used coagulation liquid for sodium alginate is a calcium chloride solution at concentration levels of 0.5% to 10% by weight. A variety of reactants in the slurry flowing through nozzle 12 and in the coagulation vessel 17 may be used. This may include other polysaccharides and other cross-linking compounds such as polyvinyl alcohol or borate fluids.
[0030] The diameter of nozzle 12, the viscosity of slurry 15, the ceramic particle content of slurry 15, pressure to feed the slurry to the nozzle, along with the frequency and amplitude of vibration applied by vibrator source 17 are adjusted to produce droplets having a desired size.
These variables are preferably set at a constant value as spheres are produced to be formed into a batch of pellets of propping material. Different batches may be produced having different size pellets. Preferably, each batch will be monosized (i.e.
contained on a single sieve such as passing through a 20 mesh sieve but staying on a 25 mesh sieve).
The pressure used to feed slurry to the nozzle is adjusted to create laminar flow through the nozzle. The feed pressure can range from 1 to 50 psi. The frequency is adjusted for each set of slurry conditions such that a resonance is established in the slurry stream exiting the nozzle that then produces spherical droplets. The frequency can range from 10 to 20,000 Hz. The pressure and frequency are optimized iteratively to create uniform spherical shapes. The Date Recue/Date Received 2021-05-05 amplitude is adjusted to improve the uniform shape of the spherical droplets formed. The flow rate of the slurry through a nozzle is a function of the nozzle diameter, slurry feed pressure, and the slurry properties such as viscosity and density. For example, for kaolin and alumina slurries through nozzles up to 500 microns in diameter the flow rate per nozzle can range from 0.2 to 3 kg/hr.
[0031] The distance between nozzle 12 and the top of the liquid 19 in coagulation vessel 17 is selected to allow droplets to become spherical before reaching the top of the liquid. The distance can be from 1 to 20 cm, but is more typically in the range of 1 to 5 cm so as to reduce distortion of the droplet shape upon impact with the liquid surface, thereby eliminating the need for a reaction gas, foam layer, or tangentially directed reaction liquid prior to the droplets entering the coagulation vessel 17. The reactant chemical in the droplets of slurry reacts with the coagulation liquid 19 in the coagulation vessel 17 and a semi-solid surface is formed on the droplets, which helps retain the spherical shape and prevents agglomeration of the pellets. Preferably, the residence time of pellets in coagulation vessel 17 is sufficient to allow pellets to become rigid enough to prevent deformation of the spherical shape when they are removed and dried, i.e., semi-rigid. In some embodiments, pellets may fall into a coagulation liquid solution flowing vertically upward so that settling of the particle through the liquid will be retarded to produce a longer residence time in the coagulation vessel.
[0032] Particles formed using the apparatus of FIG. I are washed to remove excess coagulation agent and conveyed to other devices where they are dried and later sintered, using well known processes in the industry.
[0033] FIG. 3 illustrates a multi-nozzle apparatus, which is required to apply the process on a commercial scale. Multiple nozzles 32 are placed in vessel 30, which operates under a controlled pressure to flow slurry through the nozzles. Large numbers of nozzles are required for commercial production of proppant particles. Vessel 30 is vibrated to cause vibration of nozzles, as described above. Alternatively, variable pressure may be induced in the slurry to cause formation of uniform sized droplets. The droplets are collected as described before.
[0034] Pellets produced by the process described in FIGS. 1 ¨ 3 are near uniform in size. For example, Table 1 compares the pellet size distributions for sintered alumina proppant produced by the dry mixing process and by the drip casting process described herein, without screening of the green pellets. Without screening of the green pellets, dry mixing produces fired proppant with a distribution across six screens, whereas drip casting produces fired Date Recue/Date Received 2021-05-05 proppant substantially on one screen. Therefore, in a manufacturing process for proppant, drip casting does not require sieving the green pellets to select the size range desired and then recycling the material in green pellets outside the selected size range. The size pellets to be sintered into proppant are selected by controlling the diameter of nozzle 12 or 32, the viscosity of slurry 15, the ceramic particle content of slurry 15, pressure to feed the slurry to the nozzle, along with the frequency and amplitude of vibration applied by vibrator source 17.
Table 1 ¨ Sieve Distribution of Sintered Pellets Formed by Dry Mixing and Drip casting Pan Mesh Mesh Mesh Mesh Mesh Mesh Mesh Dry 0% 17.8% 23.9% 24.3% 18.4% 10.6% 4.9% 0%
Mixing Drip 0% 0% 0.2% 99.8% 0% 0% 0% 0%
casting [0035] FIGS. 4(a-e) show photographs of aluminum oxide, bauxite, and kaolin particles produced by the apparatus of FIG 1 and by prior art methods. FIG. 4(a) shows an alumina particle made by drip casting, as illustrated in FIG. 1, which has high sphericity and a very smooth surface. FIG. 4(b) shows an alumina particle made by an Eirich mixer.
The surfaces of the particles are rough and the shapes are generally oblate. FIG. 4(c) shows a bauxite particle made by drip casting and FIG. 4(d) shows a bauxite particle made by a commercial prior art process using an Eirich mixer (Carbo HSP, sold by Carbo Ceramics Inc., Houston, TX). FIG. 4(e) shows a kaolin particle made by drip casting and FIG. 4(f) shows a kaolin particle made by a pilot scale fluidized bed process.
[0036] The surface roughness of each whole pellet shown in FIGS. 4(a-f) was measured. A
smooth, convex perimeter was drawn around each pellet, establishing an average surface level that mimicked the actual pellet surface as closely as possible while still remaining convex. Then the separation between the actual surface and the smooth, average surface was measured around the entire perimeter at intervals of 100Rm. At 100x magnification used in FIG. 4, the separation could be measured with a precision of about 0.5ttm. The average of the measurements from the entire perimeter is representative of the surface roughness of the pellet. Table 2 shows that pellets formed by dry mixing and spray fluidized bed have surface roughness from three to seven times as large as their drip cast counterparts.
Date Recue/Date Received 2021-05-05 Table 2 ¨ Surface Roughness of Drip cast and Conventionally-Formed Pellets Average Surface Roughness (um) Drip cast Alumina (FIG. 4a) 1.4 Dry Mixing-Formed Alumina (FIG. 4b) 5.8 Drip cast Bauxite (FIG. 4c) 1.6 Dry Mixing-Formed Bauxite (FIG. 4d) 4.9 Drip cast Kaolin (FIG. 4e) 0.8 Spray Fluid Bed-Formed Kaolin (FIG. 41) 5.7 [0037] FIG. 5 compares the permeability of pellets formed in the apparatus of FIG.1 compared with pellets formed by the dry mixing process. The pellets from the two processes are identical in size and composition both being a high purity (99+%) alumina.
The only variable is the pellet formation process. The permeabilities were measured in accordance with ISO 13503-5: "Procedures for Measuring the Long-term Conductivity of Proppants,"
except that steel wafers were used rather than sandstone wafers. The long term conductivity apparatus described in ISO 13503-5 utilizes a steel conductivity cell that contains an internal slot of dimensions 7 inches in length by 1.5 inches in width. An open port is placed in the cell extending from the each end of the slot to the exterior of the cell to allow for fluid flow through the slot. Other ports are placed along the length of the slot also extending to the exterior of the cell for the measurement of the internal pressure of the slot.
Into this slot are fitted a lower and upper piston the lengths which extend out beyond the dimensions of the cell such that a load may be applied directly to the pistons by a hydraulic load frame. To load the conductivity cell for the measurement of conductivity the lower piston is first secured into the cell so as not to obstruct the fluid or pressure ports. A seal ring is installed to prevent pressure or fluid leakage between slot and the piston wall. A slot sized metal shim and a sandstone wafer are then placed on the lower piston. Alternatively a steel wafer may replace the sandstone wafer (as was the case here). A set amount of proppant is then placed on the wafer. In this case equal volumes of the two proppants were loaded representing initial pack widths of about 0.19 inches. The proppant is leveled. Then on top of the proppant is placed a second steel wafer, metal shim, seal ring, and the upper piston. An initial load is applied to the pistons and fluid is flowed through the proppant pack while pressure is measured. The temperature of the fluid and cell was maintained at 250 degrees F. Measurement of the rate of fluid flow and pressure loss provides a measure of the proppant pack conductivity in Date Recue/Date Received 2021-05-05 millidarcy- feet. The permeability of the proppant pack is calculated by dividing the conductivity by the measured width of the pack, which was about 0.16 ¨ 0.19 inch for the data shown in FIG. 5. The flowing fluid was a silica saturated deoxygenated aqueous solution of 2% KC1. Conductivity was measured at stresses of 2000 psi to 20,000 psi in increments of 2000 psi. In each case the stress was held for 50 hours before measuring the conductivity. Permeability of a proppant pack decreases as closure stress increases due to failure of the proppant grains. Stronger pellets will result in a higher permeability. As can be seen in FIG. 5, pellets made by dry mixing (line 2) lose 78% of their permeability as the closure stress increases from 2000 psi to 20,000 psi. By contrast the pellets made from the apparatus in FIG. 1 (line 1) lose only 31% of their permeability ¨ less than one half of the permeability loss of the pellets made by dry mixing. This higher permeability of the pellets made from the apparatus of FIG.1 is due to the improved strength of the pellet.
[0038] The strength of a proppant can be indicated from the proppant crush resistance test described in ISO 13503-2: "Measurement of Properties of Proppants Used in Hydraulic Fracturing and Gravel-packing Operations." In this test a sample of proppant is first sieved to remove any fines (undersized pellets or fragments that may be present), then placed in a crush cell where a piston then used to apply a confined closure stress of some magnitude above the failure point of some fraction of the proppant pellets. The sample is then re-sieved and weight per cent of fines generated as a result of pellet failure is reported as percent crush. A
comparison the percent crush of two equally sized samples is a method of gauging the relative strength. For the two samples of pellets used in the conductivity test described above the weight percent crush at 15,000 psi of the pellets produced by dry mixing was 2.7% as compared to 0.8% for the drip cast pellets. This again indicates that drip casting produces a stronger pellet.
[0039] Relative pellet strength can also be determined from single pellet strength measurements. Strength distributions of forty pellets from each of the two samples of pellets used in the conductivity test described above were measured, tabulated, and analyzed using Weibull statistics for the determination of a characteristic strength. The characteristic strength of the drip cast pellets so determined was 184 MPa as compared to 151 MPa for the pellets made by dry mixing.
[0040] Fracture mechanics teaches that pellets fail under stress from the largest flaw in the pellet. In proppant pellets, the largest flaw is believed to be the largest pore. Therefore, the stress at failure is inversely proportional to the square root of the size of the largest flaw. So, Date Recue/Date Received 2021-05-05 the ratio (R) of the stress at failure of a drip cast proppant (DC) formed by the apparatus disclosed herein to a conventionally (CONY) made proppant (dry mixing or spray fluid bed processes) would be:
R = (Max pore sizenmp/Max pore sizecoN0112 [0041] Pellets made by the drip casting process and prior art processes were examined by a scanning electron microscope (SEM) at a magnification of 500x. To measure pore size distribution in particles, cross-sections of sintered alumina, bauxite and kaolin pellets made by each process were examined in the SEM. For each sample, a random area of approximately 252 ,tin x 171 gm from each of ten different pellets was photographed. The ten largest pores in each area were measured and the equation above was used to calculate the theoretical ratio of stress at failure of drip cast pellets versus conventionally made pellets.
The results are presented in Table 3. For example, the average maximum pore size in the drip cast alumina pellets was 16.3 m and for the dry mixing process alumina pellets average maximum pore size was 40.8 um. Using the equation above, the ratio of the stress to failure of the drip cast pellets to the dry mixing process pellets is 1.6. Thus fracture mechanics predicts that drip cast high alumina pellets should withstand approximately 1.6 times more stress without fracturing than dry mixing process made pellets.
Table 3 ¨ Pore Sizes of Pellets Formed by Drip casting, Dry Mixing, and Spray Fluid Bed Alumina Bauxite Kaolin Spray Dry Dry Drip cast Drip cast Drip cast Fluid Mixed Mixed Bed Average Largest Pore 16.3 40.8 14.3 37.5 11.1 56.0 (ilm) Average of 10 Largest 10.4 19.1 9.1 20.5 6.0 18.4 Pores (um) Theoretical Ratio of Drip cast Strength to 1.6x 1.6x 2.2 Conventional Strength [0042] Additional measurements were carried out on the kaolin samples. In these, every visible pore was measured and the composite data from all ten areas was used to calculate average pore size, standard deviation in pore size, and number of pores per square millimeter,
Primarily, it has been used in the food and pharmaceuticals industries. The drip casting process is Date Recue/Date Received 2021-05-05 described on the website and in sales literature of Brace GmbH. Examples of "microspheres"
formed by drip casting of different materials are also provided. U.S. Pat. No.
6,197,073 discloses a process for producing aluminum oxide beads from an acid aluminum oxide sol or acid aluminum oxide suspension by flowing the suspension through a vibrating nozzle plate to form droplets and pre-solidifying the droplets with gaseous ammonia and then coagulating the droplets in an ammonia solution. The mechanical strength of ceramic particles formed by sintering the drip cast particles was not a factor in any of the materials used in these references.
[00111 It is known that to produce ceramic proppant particles having maximum strength for a given ceramic material, the particles must contain minimum porosity, and the pores present must be kept as small as possible, since the strength of a given proppant particle is limited by its largest pore. What is needed is a method of forming green ceramic particles that can be fired to have reduced pore size and therefore maximum strength for use as a proppant.
Preferably, the particles should be spherical, have a smooth surface and have uniform size. A
method for forming the green particles without recycling of the undesired size fraction of green ceramic pellets is also needed.
BRIEF SUMMARY OF THE INVENTION
[0012] A method for forming proppant pellets from a slurry of ceramic raw materials is provided. The pellets produced have superior strength to prior proppant pellets made from a variety of ceramic raw materials using prior art pellet-forming methods.
Uniform sized spherical pellets having a smooth surface may be made in commercial quantities. The particles are used in hydraulic fracturing treatments of wells.
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S) [0013] FIG. 1 is a sketch showing the principles of the pellet-forming apparatus for proppant pellets disclosed herein.
[0014] FIG. 2 is a sketch showing a single nozzle forming droplets from a slurry stream.
[0015] FIG. 3 is a sketch showing a multi-nozzle plate forming droplets from a slurry stream.
[0016] FIG. 4a is a showing of an alumina particle made of drip casting.
[0017] FIG. 4b is a showing of an alumina particle made by an Eirich mixer.
[0018] FIG. 4c is a showing of a bauxite particle made by drip casting.
[0019] FIG. 4d is a showing of a bauxite particle made by an Eirich mixer.
Date Recue/Date Received 2021-05-05 [0020] FIG. 4e shows a kaolin particle made by drip casting.
[0021] FIG. 4f shows a kaolin particle made by a scale fluidized bed process.
[0022] FIG. 5 is a graph of long term permeability as a function of stress of alumina pellets formed by the pellet-forming apparatus disclosed herein and by the prior art dry mixing process using an Eirich mixer.
[0023] FIG. 6 is a frequency plot of pore size for particles of kaolin made by the method disclosed herein and by the prior art spray fluidized bed method.
[0024] FIG. 7 is a graph of long term permeability data for proppant having different alumina contents and made by different processes.
[0025] FIG. 8 is a graph of long-term permeability data for proppant having different alumina contents and made by different processes.
DETAILED DESCRIPTION
[0026] Referring to FIG. 1, pellet-forming apparatus 10 having a single nozzle is shown to illustrate the principles of the method disclosed herein, which is commonly called "drip casting." Nozzle 12 receives slurry 15from feed tank 14, which contains the ceramic raw materials suspended in water. Pressure applied to feed tank 14 by pressure supply system 16 causes slurry to flow through nozzle 12 at a selected rate ¨
preferably in laminar flow. Below nozzle 12 is coagulation vessel 17, which receives the droplets.
Vibrator unit 18 is connected to nozzle 12 and is used to supply pressure pulses to the nozzle or directly in the slurry flowing to the nozzle. The resulting vibration of the slurry flow through the nozzle causes the stream exiting the nozzle 12 to break into droplets of unifoun size. As droplets fall toward coagulation vessel 17, surface tension effects tend to form the droplets into spheres. Spherical particles are formed without the necessity of a sol-gel reaction, reaction gas free fall zone, foamed layer of reaction liquid or reaction liquid directed onto the droplets prior to entering the reaction liquid bath.
[0027] FIG. 2 shows details of slurry 15 exiting nozzle 12 and breaking into drops. Surface tension of the slurry drives the drops toward minimum surface area, which is acquired in a spherical shape, as they fall toward coagulation vessel 17. The distance of fall is preferably selected to be great enough to allow the droplets to become spherical before entering a liquid in vessel 17.
[0028] Slurry 15 from feed tank 14 contains a finely ground (0.01 ¨ 50 microns in size) mineral or processed powder capable of producing a strong ceramic material after sintering, a Date Recue/Date Received 2021-05-05 proper amount of dispersant necessary for keeping the solid particles in the slurry well separated, water, and a reactant that will react with a component in liquid 19 in coagulation vessel 17 to form a semi-solid or insoluble compound. The solids content of the slurries may range from about 25% to about 75%. The viscosity of the slurries will normally be from 1 to 1,000 centipoise, but may be higher. Lower viscosity of the slurry aids in improving droplet formation and formation of spherical particles and is an essential part of the invention claimed. Optimization of the dispersant type and concentration will reduce viscosity.
Dispersants may be selected based on cost, availability and effectiveness in reducing viscosity of a selected slurry. Dispersants that may be used to reduce the viscosity of slurries include sodium silicate, ammonium polyacrylate, sodium polymethacrylate, sodium citrate sodium polysulfonate and hexametaphosphate.
[0029] The commonly used reactant chemical in the slurry in feed tank 14 is sodium alginate.
This is a naturally occurring polysaccharide that is soluble in water as the sodium salt but is cross-linked to form a gel as the calcium salt. Alginate is typically added to the slurry at levels of 0.1% to 1.0% (weight percent alginate solid to total slurry).
Coagulation tank 17 normally contains a coagulation liquid 19 which gels the reactant chemical in the slurry 15.
The commonly used coagulation liquid for sodium alginate is a calcium chloride solution at concentration levels of 0.5% to 10% by weight. A variety of reactants in the slurry flowing through nozzle 12 and in the coagulation vessel 17 may be used. This may include other polysaccharides and other cross-linking compounds such as polyvinyl alcohol or borate fluids.
[0030] The diameter of nozzle 12, the viscosity of slurry 15, the ceramic particle content of slurry 15, pressure to feed the slurry to the nozzle, along with the frequency and amplitude of vibration applied by vibrator source 17 are adjusted to produce droplets having a desired size.
These variables are preferably set at a constant value as spheres are produced to be formed into a batch of pellets of propping material. Different batches may be produced having different size pellets. Preferably, each batch will be monosized (i.e.
contained on a single sieve such as passing through a 20 mesh sieve but staying on a 25 mesh sieve).
The pressure used to feed slurry to the nozzle is adjusted to create laminar flow through the nozzle. The feed pressure can range from 1 to 50 psi. The frequency is adjusted for each set of slurry conditions such that a resonance is established in the slurry stream exiting the nozzle that then produces spherical droplets. The frequency can range from 10 to 20,000 Hz. The pressure and frequency are optimized iteratively to create uniform spherical shapes. The Date Recue/Date Received 2021-05-05 amplitude is adjusted to improve the uniform shape of the spherical droplets formed. The flow rate of the slurry through a nozzle is a function of the nozzle diameter, slurry feed pressure, and the slurry properties such as viscosity and density. For example, for kaolin and alumina slurries through nozzles up to 500 microns in diameter the flow rate per nozzle can range from 0.2 to 3 kg/hr.
[0031] The distance between nozzle 12 and the top of the liquid 19 in coagulation vessel 17 is selected to allow droplets to become spherical before reaching the top of the liquid. The distance can be from 1 to 20 cm, but is more typically in the range of 1 to 5 cm so as to reduce distortion of the droplet shape upon impact with the liquid surface, thereby eliminating the need for a reaction gas, foam layer, or tangentially directed reaction liquid prior to the droplets entering the coagulation vessel 17. The reactant chemical in the droplets of slurry reacts with the coagulation liquid 19 in the coagulation vessel 17 and a semi-solid surface is formed on the droplets, which helps retain the spherical shape and prevents agglomeration of the pellets. Preferably, the residence time of pellets in coagulation vessel 17 is sufficient to allow pellets to become rigid enough to prevent deformation of the spherical shape when they are removed and dried, i.e., semi-rigid. In some embodiments, pellets may fall into a coagulation liquid solution flowing vertically upward so that settling of the particle through the liquid will be retarded to produce a longer residence time in the coagulation vessel.
[0032] Particles formed using the apparatus of FIG. I are washed to remove excess coagulation agent and conveyed to other devices where they are dried and later sintered, using well known processes in the industry.
[0033] FIG. 3 illustrates a multi-nozzle apparatus, which is required to apply the process on a commercial scale. Multiple nozzles 32 are placed in vessel 30, which operates under a controlled pressure to flow slurry through the nozzles. Large numbers of nozzles are required for commercial production of proppant particles. Vessel 30 is vibrated to cause vibration of nozzles, as described above. Alternatively, variable pressure may be induced in the slurry to cause formation of uniform sized droplets. The droplets are collected as described before.
[0034] Pellets produced by the process described in FIGS. 1 ¨ 3 are near uniform in size. For example, Table 1 compares the pellet size distributions for sintered alumina proppant produced by the dry mixing process and by the drip casting process described herein, without screening of the green pellets. Without screening of the green pellets, dry mixing produces fired proppant with a distribution across six screens, whereas drip casting produces fired Date Recue/Date Received 2021-05-05 proppant substantially on one screen. Therefore, in a manufacturing process for proppant, drip casting does not require sieving the green pellets to select the size range desired and then recycling the material in green pellets outside the selected size range. The size pellets to be sintered into proppant are selected by controlling the diameter of nozzle 12 or 32, the viscosity of slurry 15, the ceramic particle content of slurry 15, pressure to feed the slurry to the nozzle, along with the frequency and amplitude of vibration applied by vibrator source 17.
Table 1 ¨ Sieve Distribution of Sintered Pellets Formed by Dry Mixing and Drip casting Pan Mesh Mesh Mesh Mesh Mesh Mesh Mesh Dry 0% 17.8% 23.9% 24.3% 18.4% 10.6% 4.9% 0%
Mixing Drip 0% 0% 0.2% 99.8% 0% 0% 0% 0%
casting [0035] FIGS. 4(a-e) show photographs of aluminum oxide, bauxite, and kaolin particles produced by the apparatus of FIG 1 and by prior art methods. FIG. 4(a) shows an alumina particle made by drip casting, as illustrated in FIG. 1, which has high sphericity and a very smooth surface. FIG. 4(b) shows an alumina particle made by an Eirich mixer.
The surfaces of the particles are rough and the shapes are generally oblate. FIG. 4(c) shows a bauxite particle made by drip casting and FIG. 4(d) shows a bauxite particle made by a commercial prior art process using an Eirich mixer (Carbo HSP, sold by Carbo Ceramics Inc., Houston, TX). FIG. 4(e) shows a kaolin particle made by drip casting and FIG. 4(f) shows a kaolin particle made by a pilot scale fluidized bed process.
[0036] The surface roughness of each whole pellet shown in FIGS. 4(a-f) was measured. A
smooth, convex perimeter was drawn around each pellet, establishing an average surface level that mimicked the actual pellet surface as closely as possible while still remaining convex. Then the separation between the actual surface and the smooth, average surface was measured around the entire perimeter at intervals of 100Rm. At 100x magnification used in FIG. 4, the separation could be measured with a precision of about 0.5ttm. The average of the measurements from the entire perimeter is representative of the surface roughness of the pellet. Table 2 shows that pellets formed by dry mixing and spray fluidized bed have surface roughness from three to seven times as large as their drip cast counterparts.
Date Recue/Date Received 2021-05-05 Table 2 ¨ Surface Roughness of Drip cast and Conventionally-Formed Pellets Average Surface Roughness (um) Drip cast Alumina (FIG. 4a) 1.4 Dry Mixing-Formed Alumina (FIG. 4b) 5.8 Drip cast Bauxite (FIG. 4c) 1.6 Dry Mixing-Formed Bauxite (FIG. 4d) 4.9 Drip cast Kaolin (FIG. 4e) 0.8 Spray Fluid Bed-Formed Kaolin (FIG. 41) 5.7 [0037] FIG. 5 compares the permeability of pellets formed in the apparatus of FIG.1 compared with pellets formed by the dry mixing process. The pellets from the two processes are identical in size and composition both being a high purity (99+%) alumina.
The only variable is the pellet formation process. The permeabilities were measured in accordance with ISO 13503-5: "Procedures for Measuring the Long-term Conductivity of Proppants,"
except that steel wafers were used rather than sandstone wafers. The long term conductivity apparatus described in ISO 13503-5 utilizes a steel conductivity cell that contains an internal slot of dimensions 7 inches in length by 1.5 inches in width. An open port is placed in the cell extending from the each end of the slot to the exterior of the cell to allow for fluid flow through the slot. Other ports are placed along the length of the slot also extending to the exterior of the cell for the measurement of the internal pressure of the slot.
Into this slot are fitted a lower and upper piston the lengths which extend out beyond the dimensions of the cell such that a load may be applied directly to the pistons by a hydraulic load frame. To load the conductivity cell for the measurement of conductivity the lower piston is first secured into the cell so as not to obstruct the fluid or pressure ports. A seal ring is installed to prevent pressure or fluid leakage between slot and the piston wall. A slot sized metal shim and a sandstone wafer are then placed on the lower piston. Alternatively a steel wafer may replace the sandstone wafer (as was the case here). A set amount of proppant is then placed on the wafer. In this case equal volumes of the two proppants were loaded representing initial pack widths of about 0.19 inches. The proppant is leveled. Then on top of the proppant is placed a second steel wafer, metal shim, seal ring, and the upper piston. An initial load is applied to the pistons and fluid is flowed through the proppant pack while pressure is measured. The temperature of the fluid and cell was maintained at 250 degrees F. Measurement of the rate of fluid flow and pressure loss provides a measure of the proppant pack conductivity in Date Recue/Date Received 2021-05-05 millidarcy- feet. The permeability of the proppant pack is calculated by dividing the conductivity by the measured width of the pack, which was about 0.16 ¨ 0.19 inch for the data shown in FIG. 5. The flowing fluid was a silica saturated deoxygenated aqueous solution of 2% KC1. Conductivity was measured at stresses of 2000 psi to 20,000 psi in increments of 2000 psi. In each case the stress was held for 50 hours before measuring the conductivity. Permeability of a proppant pack decreases as closure stress increases due to failure of the proppant grains. Stronger pellets will result in a higher permeability. As can be seen in FIG. 5, pellets made by dry mixing (line 2) lose 78% of their permeability as the closure stress increases from 2000 psi to 20,000 psi. By contrast the pellets made from the apparatus in FIG. 1 (line 1) lose only 31% of their permeability ¨ less than one half of the permeability loss of the pellets made by dry mixing. This higher permeability of the pellets made from the apparatus of FIG.1 is due to the improved strength of the pellet.
[0038] The strength of a proppant can be indicated from the proppant crush resistance test described in ISO 13503-2: "Measurement of Properties of Proppants Used in Hydraulic Fracturing and Gravel-packing Operations." In this test a sample of proppant is first sieved to remove any fines (undersized pellets or fragments that may be present), then placed in a crush cell where a piston then used to apply a confined closure stress of some magnitude above the failure point of some fraction of the proppant pellets. The sample is then re-sieved and weight per cent of fines generated as a result of pellet failure is reported as percent crush. A
comparison the percent crush of two equally sized samples is a method of gauging the relative strength. For the two samples of pellets used in the conductivity test described above the weight percent crush at 15,000 psi of the pellets produced by dry mixing was 2.7% as compared to 0.8% for the drip cast pellets. This again indicates that drip casting produces a stronger pellet.
[0039] Relative pellet strength can also be determined from single pellet strength measurements. Strength distributions of forty pellets from each of the two samples of pellets used in the conductivity test described above were measured, tabulated, and analyzed using Weibull statistics for the determination of a characteristic strength. The characteristic strength of the drip cast pellets so determined was 184 MPa as compared to 151 MPa for the pellets made by dry mixing.
[0040] Fracture mechanics teaches that pellets fail under stress from the largest flaw in the pellet. In proppant pellets, the largest flaw is believed to be the largest pore. Therefore, the stress at failure is inversely proportional to the square root of the size of the largest flaw. So, Date Recue/Date Received 2021-05-05 the ratio (R) of the stress at failure of a drip cast proppant (DC) formed by the apparatus disclosed herein to a conventionally (CONY) made proppant (dry mixing or spray fluid bed processes) would be:
R = (Max pore sizenmp/Max pore sizecoN0112 [0041] Pellets made by the drip casting process and prior art processes were examined by a scanning electron microscope (SEM) at a magnification of 500x. To measure pore size distribution in particles, cross-sections of sintered alumina, bauxite and kaolin pellets made by each process were examined in the SEM. For each sample, a random area of approximately 252 ,tin x 171 gm from each of ten different pellets was photographed. The ten largest pores in each area were measured and the equation above was used to calculate the theoretical ratio of stress at failure of drip cast pellets versus conventionally made pellets.
The results are presented in Table 3. For example, the average maximum pore size in the drip cast alumina pellets was 16.3 m and for the dry mixing process alumina pellets average maximum pore size was 40.8 um. Using the equation above, the ratio of the stress to failure of the drip cast pellets to the dry mixing process pellets is 1.6. Thus fracture mechanics predicts that drip cast high alumina pellets should withstand approximately 1.6 times more stress without fracturing than dry mixing process made pellets.
Table 3 ¨ Pore Sizes of Pellets Formed by Drip casting, Dry Mixing, and Spray Fluid Bed Alumina Bauxite Kaolin Spray Dry Dry Drip cast Drip cast Drip cast Fluid Mixed Mixed Bed Average Largest Pore 16.3 40.8 14.3 37.5 11.1 56.0 (ilm) Average of 10 Largest 10.4 19.1 9.1 20.5 6.0 18.4 Pores (um) Theoretical Ratio of Drip cast Strength to 1.6x 1.6x 2.2 Conventional Strength [0042] Additional measurements were carried out on the kaolin samples. In these, every visible pore was measured and the composite data from all ten areas was used to calculate average pore size, standard deviation in pore size, and number of pores per square millimeter,
- 11 -Date Recue/Date Received 2021-05-05 as well as the largest pore data, which are presented in Table 3. A summary of the data is presented in Table 4, and FIG. 6 shows plots of the pore size distributions for drip cast kaolin (Curve 1) and spray fluid bed kaolin (Curve 2). The small percentage of very large pores generated by the spray fluid bed process shown in FIG. 6 (Curve 2) are readily visible in the microstructures in FIG. 4f. The lack of large pores in the drip cast material provides the strength advantage discussed above.
Table 4 ¨ Additional Pore Size Measurements for Drip cast and Spray Fluid Bed Kaolin Drip cast Kaolin Spray Fluid Bed Kaolin Average Pore Size ( m) 2.0 2.8 Standard Deviation in Pore Size (tm) 1.8 6.4 Average Number of Pores Per Square Millimeter [0043] Proppant made from kaolin has a cost advantage over proppants containing higher alumina contents, which are made from higher-cost ores containing higher percentages of alumina. Four proppant products having three ranges of alumina content are sold by Carbo Ceramics, for example (data from www.carboceramics.com , searched 12/19/2011).
Higher alumina content proppants generally sell for higher prices and cost more to manufacture. The lowest alumina contents are in the products ECONOPROP and CARBOLITE, in which the alumina content is about 48 and 51 per cent, respectively. A higher alumina content is in CARBOPROP, in which the alumina content is about 72 per cent. The CARBOPROP is a more expensive product to make primarily because of higher raw material costs.
[0044] The property of a proppant that is most directly related to its performance in hydraulic fractures is permeability under stress. Long-term permeability data for pure alumina proppant made by a prior art method and by the drip-casting process disclosed herein are shown in FIG. 5. FIG. 7 shows long-term permeability data, measured using the same procedures as used to obtain the data in FIG. 5, for proppant having different alumina contents and made by different processes. Curve 1 represents published permeability of 20/40 mesh ECONOPROP proppant (made from kaolin, having an alumina content of about 48 per cent) made by the Eirich-mixer process described above. Curve 2 represents permeability of 20/40 mesh CARBOPROP proppant (made from a mixture of ores having an alumina content of about 72 per cent). Curve 3 represents the average permeability vs stress of 15 samples of proppant (made from kaolin, having an alumina content of about 48 per
Table 4 ¨ Additional Pore Size Measurements for Drip cast and Spray Fluid Bed Kaolin Drip cast Kaolin Spray Fluid Bed Kaolin Average Pore Size ( m) 2.0 2.8 Standard Deviation in Pore Size (tm) 1.8 6.4 Average Number of Pores Per Square Millimeter [0043] Proppant made from kaolin has a cost advantage over proppants containing higher alumina contents, which are made from higher-cost ores containing higher percentages of alumina. Four proppant products having three ranges of alumina content are sold by Carbo Ceramics, for example (data from www.carboceramics.com , searched 12/19/2011).
Higher alumina content proppants generally sell for higher prices and cost more to manufacture. The lowest alumina contents are in the products ECONOPROP and CARBOLITE, in which the alumina content is about 48 and 51 per cent, respectively. A higher alumina content is in CARBOPROP, in which the alumina content is about 72 per cent. The CARBOPROP is a more expensive product to make primarily because of higher raw material costs.
[0044] The property of a proppant that is most directly related to its performance in hydraulic fractures is permeability under stress. Long-term permeability data for pure alumina proppant made by a prior art method and by the drip-casting process disclosed herein are shown in FIG. 5. FIG. 7 shows long-term permeability data, measured using the same procedures as used to obtain the data in FIG. 5, for proppant having different alumina contents and made by different processes. Curve 1 represents published permeability of 20/40 mesh ECONOPROP proppant (made from kaolin, having an alumina content of about 48 per cent) made by the Eirich-mixer process described above. Curve 2 represents permeability of 20/40 mesh CARBOPROP proppant (made from a mixture of ores having an alumina content of about 72 per cent). Curve 3 represents the average permeability vs stress of 15 samples of proppant (made from kaolin, having an alumina content of about 48 per
- 12 -Date Recue/Date Received 2021-05-05 cent) made by the drip cast method disclosed herein. The drip cast process produces a proppant made from kaolin that has about the same permeability under stress as the higher-cost product containing 72 per cent alumina. The average long-term permeability measured at 10,000 psi stress of 15 samples was 173 darcies. This is far above the published long-term permeability at 10,000 psi stress (85 darcies) of the commercial proppant (ECONOPROP) having about the same alumina content, as can be seen by comparing Curve 3 and Curve 1.
[0045] FIG. 8 shows long-term permeability data, measured by the same procedures as used to obtain the data in FIGs, 5 and 7, for proppant having different alumina contents and made by different processes. Curve 1 represents published permeability data for 20/40 mesh CARBOPROP proppant formed by the Eirich mixer process described above (made from a mixture of ores having an alumina content of about 72 percent). Curve 2 represents permeability data for proppant (primarily sieved on a 25-mesh screen) made by the drip cast method disclosed herein using bauxite with an alumina content of 70 percent.
Curve 3 represents permeability data for 20/40 mesh proppant made by the Eirich mixer process and having an alumina content of about 83 percent alumina. The permeability of the proppant made by the drip cast method and having an alumina content of only 70 per cent exhibits practically the same permeability behavior as the prior art proppant made with an Eirich mixer and having about 83 per cent alumina. Since alumina is a more expensive component of proppants, there is considerable saving by using lower cost raw materials and the drip cast process disclosed herein. Comparison of Curves 1 and 2 shows the benefits of the drip cast process with about the same alumina content in the proppant.
[0046] It is understood that modifications to the invention may be made as might occur to one skilled in the field of the invention within the scope of the appended claims. All embodiments contemplated hereunder which achieve the objects of the invention have not been shown in complete detail. Other embodiments may be developed without departing from the spirit of the invention or from the scope of the appended claims.
Although the present invention has been described with respect to specific details, it is not intended that such details should be regarded as limitations on the scope of the invention, except to the extent that they are included in the accompanying claims.
[0045] FIG. 8 shows long-term permeability data, measured by the same procedures as used to obtain the data in FIGs, 5 and 7, for proppant having different alumina contents and made by different processes. Curve 1 represents published permeability data for 20/40 mesh CARBOPROP proppant formed by the Eirich mixer process described above (made from a mixture of ores having an alumina content of about 72 percent). Curve 2 represents permeability data for proppant (primarily sieved on a 25-mesh screen) made by the drip cast method disclosed herein using bauxite with an alumina content of 70 percent.
Curve 3 represents permeability data for 20/40 mesh proppant made by the Eirich mixer process and having an alumina content of about 83 percent alumina. The permeability of the proppant made by the drip cast method and having an alumina content of only 70 per cent exhibits practically the same permeability behavior as the prior art proppant made with an Eirich mixer and having about 83 per cent alumina. Since alumina is a more expensive component of proppants, there is considerable saving by using lower cost raw materials and the drip cast process disclosed herein. Comparison of Curves 1 and 2 shows the benefits of the drip cast process with about the same alumina content in the proppant.
[0046] It is understood that modifications to the invention may be made as might occur to one skilled in the field of the invention within the scope of the appended claims. All embodiments contemplated hereunder which achieve the objects of the invention have not been shown in complete detail. Other embodiments may be developed without departing from the spirit of the invention or from the scope of the appended claims.
Although the present invention has been described with respect to specific details, it is not intended that such details should be regarded as limitations on the scope of the invention, except to the extent that they are included in the accompanying claims.
- 13 -Date Recue/Date Received 2021-05-05
Claims (9)
1. A ceramic particle, comprising:
a sintered ceramic material;
a size of about 80 mesh to about 10 mesh;
an average largest pore size of less than about 20 microns; and a surface roughness of less than about 2 microns.
a sintered ceramic material;
a size of about 80 mesh to about 10 mesh;
an average largest pore size of less than about 20 microns; and a surface roughness of less than about 2 microns.
2. The ceramic particle of claim 1, wherein the sintered ceramic material comprises sintered alumina, sintered kaolin, or sintered bauxite.
3. The ceramic particle of claim 1, further comprising a porosity.
4. The proppant particle of claim 1, wherein the surface roughness is from about 0.8 pm to about 1.6 pm.
5. A method of hydraulic fracturing a subterranean formation, comprising:
injecting a hydraulic fluid into a subterranean formation at a rate and pressure sufficient to open a fracture therein; and injecting a fluid containing the ceramic particle of claim 1 into the fracture.
injecting a hydraulic fluid into a subterranean formation at a rate and pressure sufficient to open a fracture therein; and injecting a fluid containing the ceramic particle of claim 1 into the fracture.
6. A proppant particle, comprising:
a ceramic material selected from the group consisting of sintered bauxite, sintered kaolin, and sintered alumina, and combinations thereof;
Date Recue/Date Received 2021-05-05 wherein the proppant particle has a size of about 40 mesh to about 20 mesh and a surface roughness of from about 0.8 pm to less than about 2 pm.
a ceramic material selected from the group consisting of sintered bauxite, sintered kaolin, and sintered alumina, and combinations thereof;
Date Recue/Date Received 2021-05-05 wherein the proppant particle has a size of about 40 mesh to about 20 mesh and a surface roughness of from about 0.8 pm to less than about 2 pm.
7. The proppant particle of claim 6, wherein the surface roughness is from about 0.8 pm to about 1.6 pm.
8. The proppant particle of claim 6, further comprising a porosity.
9. The proppant particle of claim 6, further comprising a standard deviation in pore size of less than 4 pm.
Date Recue/Date Received 2021-05-05
Date Recue/Date Received 2021-05-05
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EA201790697A1 (en) * | 2014-09-30 | 2017-10-31 | Карбо Керамикс Инк. | PARTICLES OF BENDING FILLER, OBTAINED FROM DROPS SUSPENSION, AND METHODS OF APPLICATION |
WO2016077339A1 (en) * | 2014-11-10 | 2016-05-19 | Imerys Oilfield Minerals, Inc. | Method for preparing bauxite and/or kaolin for use in ceramic proppants |
CA2992942A1 (en) * | 2015-07-17 | 2017-01-26 | Carbo Ceramics Inc. | Proppant particles formed from slurry droplets and methods of use |
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CA1217319A (en) * | 1983-02-07 | 1987-02-03 | Arup K. Khaund | Low density proppant |
JPH0653805B2 (en) * | 1986-10-31 | 1994-07-20 | 鐘淵化学工業株式会社 | Method for producing disc-shaped particles |
CA1329461C (en) * | 1987-04-14 | 1994-05-17 | Alcan International Limited | Process of producing aluminum and titanium nitrides |
US20060162929A1 (en) * | 2005-01-26 | 2006-07-27 | Global Synfrac Inc. | Lightweight proppant and method of making same |
BRPI0502622A (en) * | 2005-06-24 | 2007-02-13 | Mineracao Curimbaba Ltda | spherical ceramic propellant for hydraulic fracturing of oil or gas wells and process for forming cavities on the surface of spherical ceramic propellants |
US7845409B2 (en) * | 2005-12-28 | 2010-12-07 | 3M Innovative Properties Company | Low density proppant particles and use thereof |
US20090118145A1 (en) * | 2007-10-19 | 2009-05-07 | Carbo Ceramics Inc. | Method for producing proppant using a dopant |
US7703521B2 (en) * | 2008-02-19 | 2010-04-27 | Schlumberger Technology Corporation | Polymeric microspheres as degradable fluid loss additives in oilfield applications |
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US9175210B2 (en) * | 2011-03-11 | 2015-11-03 | Carbo Ceramics Inc. | Proppant particles formed from slurry droplets and method of use |
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